Book contents
- Frontmatter
- Contents
- Introduction
- Participants
- Non-Participant Contributors
- Part 1 Transmissible diseases with long development times and vaccination strategies
- Part 2 Dynamics of immunity (development of disease within individuals)
- Evolutionary dynamics of HIV infections
- Statistical models for analysis of longitudinal, CD4 data
- Some mathematical and statistical issues in assessing the evidence for acquired immunity to schistosomiasis
- Virulence and transmissibility in P. falciparum malaria
- Invited Discussion
- Invited Discussion
- Invited Discussion
- Lifespan of human T lymphocytes
- Diversity and virulence thresholds in AIDS
- Statistical analysis of AZT effect on CD4 cell counts in HIV disease
- Modeling progression of HIV infection: staging and the Chicago MACS cohort
- The interpretation of immunoepidemiological data for helminth infections
- The distribution of malaria parasites in the mosquito vector: consequences for assessing infection intensity in the field
- When susceptible and infective human hosts are not equally attractive to mosquitoes: a generalisation of the Ross malaria model
- The dynamics of blood stage malaria: modelling strain specific and strain transcending immunity
- Part 3 Population heterogeneity (mixing)
- Part 4 Consequences of treatment interventions
- Part 5 Prediction
Statistical models for analysis of longitudinal, CD4 data
Published online by Cambridge University Press: 04 August 2010
- Frontmatter
- Contents
- Introduction
- Participants
- Non-Participant Contributors
- Part 1 Transmissible diseases with long development times and vaccination strategies
- Part 2 Dynamics of immunity (development of disease within individuals)
- Evolutionary dynamics of HIV infections
- Statistical models for analysis of longitudinal, CD4 data
- Some mathematical and statistical issues in assessing the evidence for acquired immunity to schistosomiasis
- Virulence and transmissibility in P. falciparum malaria
- Invited Discussion
- Invited Discussion
- Invited Discussion
- Lifespan of human T lymphocytes
- Diversity and virulence thresholds in AIDS
- Statistical analysis of AZT effect on CD4 cell counts in HIV disease
- Modeling progression of HIV infection: staging and the Chicago MACS cohort
- The interpretation of immunoepidemiological data for helminth infections
- The distribution of malaria parasites in the mosquito vector: consequences for assessing infection intensity in the field
- When susceptible and infective human hosts are not equally attractive to mosquitoes: a generalisation of the Ross malaria model
- The dynamics of blood stage malaria: modelling strain specific and strain transcending immunity
- Part 3 Population heterogeneity (mixing)
- Part 4 Consequences of treatment interventions
- Part 5 Prediction
Summary
Introduction
The importance of CD4 T-cells in AIDS and HIV infection has long been recognized. Measurements of the CD4 number, obtained from the peripheral blood, give an indication of the amount of immune suppression, with lower numbers indicating more severe immune deficiency. They have been shown to be of great prognostic significance for predicting clinical outcomes (Fahey et al. 1990); they are useful in patient care for monitoring an individual's health; they are used in epidemiological studies and in some countries they are used in determining the availability of health care resources and even are incorporated into the definition of AIDS. CD4 T-cell numbers are also used in determining the eligibility criteria and as stratification variables in randomised clinical trials.
In a previous paper (Taylor et al. 1994) we considered various statistical models which attempted to describe the variation in the patterns of decline of CD4 T-cell numbers in HIV infected subjects. These models were fitted to data from the Los Angeles portion of the Multicenter AIDS cohort study (MACS). One of the aims in this analysis is to investigate whether individuals maintain a fixed rate of decline of CD4 after allowing for the variability of the measurements, that is whether a subject who is following a certain path in their CD4 measurements will remain on that path in the future. One possibility is that individuals do maintain a fixed slope indefinitely, another possibility is that the future slope is unrelated to the past slope. We develop a family of models in which these two scenarios are special cases.
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- Information
- Models for Infectious Human DiseasesTheir Structure and Relation to Data, pp. 127 - 138Publisher: Cambridge University PressPrint publication year: 1996
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